A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357957



Internal ID22583626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72120903..72125248hg38UCSC Ensembl
chr11:71831949..71836294hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384346
hg194346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914646
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357957
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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